Hypercalciuria, Absorptive, 2 (HCA2)

Alias:
Hypercalciuria, Absorptive, Susceptibility to
Familial Idiopathic Hypercalciuria
Hypercalciuria, Absorptive
Hca2
Hypercalciuria, Familial Idiopathic
Hypercalciuria Familial Idiopathic
Hypercalciuria, Absorptive, Type 2
Hypercalciuria Absorptive 2
Hypercalciuria
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypercalciuria, Absorptive, 2, also known as hypercalciuria, absorptive, susceptibility to, is related to nephrolithiasis and idiopathic hypercalciuria, and has symptoms including polyuria, lower urinary tract symptoms and urological manifestations. An important gene associated with Hypercalciuria, Absorptive, 2 is ADCY10 (Adenylate Cyclase 10), and among its related pathways/superpathways is Ca, cAMP and Lipid Signaling. The drugs Cholecalciferol and Ergocalciferol have been mentioned in the context of this disorder. Affiliated tissues include bone and kidney, and related phenotypes are hypercalciuria and calcium oxalate nephrolithiasis
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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7
64
10

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Mutations
No data available

Related Drugs

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CAS Number
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No data available

Disease Model

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Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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IF
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